Secondary analysis of GenRED data (Genetics of Recurrent Early-Onset major Depression) using MERLIN

The familial relevance of depression is a critical aspect, with evidence suggesting a substantial hereditary component. Investigating the inheritance patterns within families can provide valuable insights into the genetic underpinnings of depression. To gain a new perspective on the genetics underpinning of depression, we conducted a novel analysis of the Genetics of Recurrent Early-onset Depression (GenRED) dataset including 683 U.S. Caucasian families, each with one proband with recurrent early-onset major depression and at least one sibling with depression. Using the MERLIN tool, we identified 37 genomic markers with nominal significance linkage to early-onset recurrent depression. The findings differ from prior analyses of GenRED using a different analytical tool. Our findings highlight the variability and potential discrepancies that can arise from using different analytical tools on the same dataset. Given the chance of microsatellites undergoing duplication, mutations, and amplification errors, our two-point analysis can be more robust compared to the previous multipoint analysis. Also, one limitation is genetic admixture; studies with more homogenous ethnic groups are warranted.

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Publication Details

Journal
European Archives of Psychiatry and Clinical Neuroscience
Published
2025-04-26
DOI
https://doi.org/10.1007/s00406-025-02014-y
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Secondary analysis of GenRED data (Genetics of Recurrent Early-Onset major Depression) using MERLIN

Claudia Gragnoli, Mutaz Amin
European Archives of Psychiatry and Clinical Neuroscience
Genetics and Neurodevelopmental Disorders
article

Secondary analysis of GenRED data (Genetics of Recurrent Early-Onset major Depression) using MERLIN

Claudia Gragnoli, Mutaz Amin
article en

Abstract

The familial relevance of depression is a critical aspect, with evidence suggesting a substantial hereditary component. Investigating the inheritance patterns within families can provide valuable insights into the genetic underpinnings of depression. To gain a new perspective on the genetics underpinning of depression, we conducted a novel analysis of the Genetics of Recurrent Early-onset Depression (GenRED) dataset including 683 U.S. Caucasian families, each with one proband with recurrent early-onset major depression and at least one sibling with depression. Using the MERLIN tool, we identified 37 genomic markers with nominal significance linkage to early-onset recurrent depression. The findings differ from prior analyses of GenRED using a different analytical tool. Our findings highlight the variability and potential discrepancies that can arise from using different analytical tools on the same dataset. Given the chance of microsatellites undergoing duplication, mutations, and amplification errors, our two-point analysis can be more robust compared to the previous multipoint analysis. Also, one limitation is genetic admixture; studies with more homogenous ethnic groups are warranted.

European Archives of Psychiatry and Clinical NeuroscienceVol. 276(2)
Creighton University (US), Thomas Jefferson University (US), Al-Neelain University (SD), Biotech Park (IN), Universitätsklinik für Diabetologie, Endokrinologie, Ernährungsmedizin & Metabolismus (CH), Penn State Milton S. Hershey Medical Center (US)
U.S. Department of Health and Human Services, Creighton University, Nebraska Department of Health and Human Services, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Good health and well-being
Openalex Percentile: Top 90%
Genetics and Neurodevelopmental Disorders
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